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(ii) Dmrt : The minireview of Herpin and Schartl (2011) summarizes
information thus far gathered on the early gonadal differentiation in
a dozen gonochoric fi sh. Of fi ve genes, gonad specifi c expression has
been found for Dmrt1 in many species, Dmrt2 in O. latipes (Winkler et
al., 2004), Dmrt3 in D. rerio (Li et al., 2008), Dmrt4 in O. aureus (Cao et
al., 2010), O. latipes (Winkler et al., 2004), Paralichthys olivaceus (Wen
et al., 2009) and Dmrt 5 in D. rerio (Guo et al., 2004). Interestingly,
Dmrt4 and Dmrt1 are predominantly expressed in the ovary and
testis of O. aureus, respectively. They have been sub-cloned into the
vector pMAL-c2x and introduced into the Escherichia coli TB1 cell for
effi cient fusion. After purifi cation and cleavage, Dmrt4 and Dmrt1
proteins have been used to immunize adult rabbits. Western blot
analysis has shown that these Dmrt4 and Dmrt1 have become highly
specifi c and are expressed only in the ovary and testis, respectively
(Cao et al., 2007). Male restricted expression has been shown in O.
latipes, X. maculatus, P. olivaceus, O. niloticus, Gobiocypris rarus and
Clarias gariepinus (Table 11). A strong male-biased expression has been
found in O. mykiss, D. rerio, Takifugu rubripes, Gadus morhua, Acipenser
fulvescens, Scaphirhynchus platorhynchus and Silurus meridionalis. When
detected in the ovary, the expression of Dmrt1 is specifi c to germ
cells alone in G. morhua and D. rerio. Two distinct DM domain DNAs
tDMRT1 from the testis and tDMO from the ovary are isolated in
O. niloticus . A male specifi c motif is absent in tDMO. The alternatively
spliced male and female types of double sex tDmrt-1 and tDMO cDNAs
are encoded by two different genes. The mutually exclusive nature of
tDmrt-1 and tDMO expression in the testis and ovary indicates that
they both play an important role in gonad development and function.
In vitro (promoter analysis) studies have revealed that Dmrt1 inhibits
transcriptional activity of cyp19a1a and Double sex and Mab-3 domain
is essential to repress basal as well as Ad4BP/SF-1- activated cyp19a1a
in HEK 293 cells. Immunohistochemical analysis has shown that the
transgenic overexpression of Dmrt1 in XX tilapia down- regulated
cyp19a1a expression, decreased aromatase expression reduced serum
estradiol 17β levels, retardation of the formation of ovarian cavity
induced varying degrees of follicular degeneration and even a partial
or complete sex reversal (Wang et al., 2010). In S. meridionalis too,
Dmrt1a expresses in the testis but Dmrt1b in the ovary (Liu Z et al.,
2007). In Clarias gariepinus, Raghuveer and Senthilkumaran (2009)
have found two alternative spliced forms of Dmrt1 . They code for
proteins with 287 ( Dmrt ), 253 ( Dmrt1a ) and 233 ( Dmrt1b ) amino acid
residues and are localized in spermatogonia and spermatocytes. The
potential role of Dmrt1 in testicular differentiation, as evidenced
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